Evidence map›Paper›PMID 41809114›Full record

ArticleThe journal of allergy and clinical immunology. Global2026

Severe eosinophilia and risk of major disease and mortality: A nationwide cohort study of children and adults.

Shay Nemet, Daniel Elbirt, Ramon Cohen, Keren Mahlab-Guri, Vered Shkalim Zemer, Ilan Asher, Aviv Talmon, Limor Rubin, Yaarit Ribak, Eyal Ben-Dori and 5 more

Abstract read
In one paragraph

Article in The journal of allergy and clinical immunology. Global, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Shay NemetAllergy and Clinical Immunology Unit, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Daniel ElbirtAllergy and Clinical Immunology Unit, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Ramon CohenAllergy and Clinical Immunology Unit, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Keren Mahlab-GuriAllergy and Clinical Immunology Unit, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Vered Shkalim ZemerFaculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Ilan AsherAllergy and Clinical Immunology Unit, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Aviv TalmonAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Limor RubinAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Yaarit RibakAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Eyal Ben-DoriAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Inon SarigAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Nur SagiAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Ruslan SergienkoDepartment of Health Policy and Management, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Yuval TalAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Oded ShamrizAllergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Severe eosinophilia (SE), defined as greater than 5000 cells/μL, is uncommon but may indicate serious underlying disease. Its long-term prognostic implications across age groups remain unclear. Objectives: We sought to investigate the long-term risk of morbidity and all-cause mortality in children and adults with SE. Methods: We conducted a nationwide, population-based, matched cohort study using data from Clalit Health Services, Israel (2000-2023). Individuals with SE (n = 3822) were matched 1:10 to subjects without SE with normal eosinophil counts (<500/μL; n = 39,005). Five-year risks of cancer, autoimmune disease, thromboembolic events, allergic disorders, and all-cause mortality were assessed using multivariable Cox proportional hazards models. Results: The study included 42,827 participants, both with and without SE. Among the 29,289 adults, 2,497 had SE and 26,792 did not. Among the 13,538 children, 1,325 had SE and 12,213 did not. Among adults, SE was associated with increased risk of hematologic malignancy (hazard ratio [HR], 2.86; 95% CI, 1.88-4.36), autoimmune disease (HR, 1.64; 95% CI, 1.38-1.95), thromboembolic events (HR, 1.91; 95% CI, 1.45-2.53), and mortality (HR, 2.20; 95% CI, 1.84-2.62). In children, SE predicted solid tumors (HR, 14.24; 95% CI, 2.39-85.00), autoimmune disease (HR, 2.48; 95% CI, 1.97-3.12), allergic disorders (HR, 1.45; 95% CI, 1.26-1.67), and markedly increased mortality (HR, 7.95; 95% CI, 3.23-19.56). Conclusions: Severe eosinophilia is a strong prognostic marker in both children and adults, associated with malignancy, autoimmune and thromboembolic disease, and premature death. Recognition of SE should prompt comprehensive evaluation and close follow-up in general and specialty caregivers.

Indexed as

epidemiologylong-termnationwidepopulation-basedSevere eosinophilia

Identifiers

PMID41809114
PMCPMC12968414

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.